Please choose an event type to view the corresponding MedsFacts report:

ANAEMIA ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
ASTHENIA ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
ANOREXIA ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
COMA ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
BRONCHITIS ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
FALL ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PAIN ( 5 FDA reports)
PANCREATITIS CHRONIC ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MANIA ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
COMPULSIONS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
MENINGIOMA ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
OBESITY ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANGER ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENINGITIS HERPES ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
PRESBYOPIA ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THYROID GLAND CANCER ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGITIS CHEMICAL ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL FUNCTION TEST ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETCHING ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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